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  2. Conjunction elimination - Wikipedia

    en.wikipedia.org/wiki/Conjunction_elimination

    In propositional logic, conjunction elimination (also called and elimination, ∧ elimination, [1] or simplification) [2][3][4] is a valid immediate inference, argument form and rule of inference which makes the inference that, if the conjunction A and B is true, then A is true, and B is true. The rule makes it possible to shorten longer proofs ...

  3. Terpene - Wikipedia

    en.wikipedia.org/wiki/Terpene

    The term terpene was coined in 1866 by the German chemist August Kekulé to denote all hydrocarbons having the empirical formula C 10 H 16, of which camphene was one. Previously, many hydrocarbons having the empirical formula C 10 H 16 had been called "camphene", but many other hydrocarbons of the same composition had had different names.

  4. Hammond's postulate - Wikipedia

    en.wikipedia.org/wiki/Hammond's_postulate

    George Hammond developed the postulate during his professorship at Iowa State University. Hammond's postulate (or alternatively the Hammond–Leffler postulate), is a hypothesis in physical organic chemistry which describes the geometric structure of the transition state in an organic chemical reaction. [1] First proposed by George Hammond in ...

  5. Syn and anti addition - Wikipedia

    en.wikipedia.org/wiki/Syn_and_anti_addition

    Syn and anti addition. In organic chemistry, syn- and anti-addition are different ways in which substituent molecules can be added to an alkene (R2C=CR2) or alkyne (RC≡CR). The concepts of syn and anti addition are used to characterize the different reactions of organic chemistry by reflecting the stereochemistry of the products in a reaction.

  6. Michael addition reaction - Wikipedia

    en.wikipedia.org/wiki/Michael_Addition_Reaction

    Michael addition reaction. In organic chemistry, the Michael reaction or Michael 1,4 addition is a reaction between a Michael donor (an enolate or other nucleophile) and a Michael acceptor (usually an α,β-unsaturated carbonyl) to produce a Michael adduct by creating a carbon-carbon bond at the acceptor's β-carbon. [1][2] It belongs to the ...

  7. Elimination reaction - Wikipedia

    en.wikipedia.org/wiki/Elimination_reaction

    An elimination reaction is a type of organic reaction in which two substituents are removed from a molecule in either a one- or two-step mechanism. [2] The one-step mechanism is known as the E2 reaction, and the two-step mechanism is known as the E1 reaction. The numbers refer not to the number of steps in the mechanism, but rather to the ...

  8. Modus ponens - Wikipedia

    en.wikipedia.org/wiki/Modus_ponens

    In propositional logic, modus ponens (/ ˈ m oʊ d ə s ˈ p oʊ n ɛ n z /; MP), also known as modus ponendo ponens (from Latin 'method of putting by placing'), [1] implication elimination, or affirming the antecedent, [2] is a deductive argument form and rule of inference. [3] It can be summarized as "P implies Q. P is true. Therefore, Q must ...

  9. Cope rearrangement - Wikipedia

    en.wikipedia.org/wiki/Cope_rearrangement

    RXNO:0000028. The Cope rearrangement is an extensively studied organic reaction involving the [3,3]-sigmatropic rearrangement of 1,5- dienes. [1][2][3][4] It was developed by Arthur C. Cope and Elizabeth Hardy. For example, 3-methyl-hexa-1,5-diene heated to 300 °C yields hepta-1,5-diene. The Cope rearrangement causes the fluxional states of ...

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